Novel mitochondrial DNA mutations in a rare variety of hypertrophic cardiomyopathy.
Int J Cardiol
; 109(3): 432-3, 2006 May 24.
Article
em En
| MEDLINE
| ID: mdl-16266762
ABSTRACT
We report a rare case of a 65 year old male with mid left ventricular cavity obstruction which is an uncommon form of hypertrophic cardiomyopathy with cytogenetic analysis revealing novel mutations in mitochondrial nucleic acid.
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Base de dados:
MEDLINE
Assunto principal:
Cardiomiopatia Hipertrófica
/
DNA Mitocondrial
/
Mutação
Idioma:
En
Ano de publicação:
2006
Tipo de documento:
Article